| Primary Device ID | 00380659909467 |
| NIH Device Record Key | 0d3a82fc-6ed1-4969-8950-0c87bab08972 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Alcon AcrySof® |
| Version Model Number | Version 3 |
| Company DUNS | 008018525 |
| Company Name | Alcon Laboratories, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com | |
| Phone | +18008625266 |
| web.masterus@alcon.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00380659909467 [Primary] |
| HQL | intraocular lens |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-06-07 |
| Device Publish Date | 2016-12-13 |
| 00380650500045 - EX-PRESS | 2025-10-01 EX-PRESS Glaucoma Filtration Device - Version P-50 |
| 00380652432085 - Clareon | 2025-04-22 CLAREON TORIC UVA |
| 00380652432092 - Clareon | 2025-04-22 CLAREON TORIC UVA |
| 00380652432108 - Clareon | 2025-04-22 CLAREON TORIC UVA |
| 00380652432115 - Clareon | 2025-04-22 CLAREON TORIC UVA |
| 00380652433143 - Clareon | 2025-04-22 CLAREON TORIC UVA |
| 00380652433150 - Clareon | 2025-04-22 CLAREON TORIC UVA |
| 00380652433167 - Clareon | 2025-04-22 CLAREON TORIC UVA |